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©The Author(s) 2025.
World J Diabetes. Mar 15, 2025; 16(3): 92003
Published online Mar 15, 2025. doi: 10.4239/wjd.v16.i3.92003
Published online Mar 15, 2025. doi: 10.4239/wjd.v16.i3.92003
Figure 3 Downregulation of lnc-MGC can mediate the protective effect of retinal pigment epithelial cells through ER stress and ferroptosis.
A: CCK-8 detection of cell proliferation activity; B: TUNEL detection of cell apoptosis. The scale bar represents 100 μm; C: ELISA detection of the expression of the inflammatory cytokines TNF-α, IL-1β and IL-6; D: Flow cytometry detection of reactive oxygen species; E: Western blotting was used to detect the expression of the apoptosis-related proteins Bax, Bcl-2 and cleaved-caspase 3; F: Western blotting was used to detect the expression of the ER-related proteins GRP78, CHOP and XBP-1; G: Western blotting was used to detect the expression of the ferroptosis-associated proteins GPX4, HO-1, FTH1, and xCT. aP < 0.05, bP < 0.01, and cP < 0.001. NC: Normal control; HG: High glucose; ROS: Reactive oxygen species.
- Citation: Luo YY, Ba XY, Wang L, Zhang YP, Xu H, Chen PQ, Zhang LB, Han J, Luo H. LEF1 influences diabetic retinopathy and retinal pigment epithelial cell ferroptosis via the miR-495-3p/GRP78 axis through lnc-MGC. World J Diabetes 2025; 16(3): 92003
- URL: https://www.wjgnet.com/1948-9358/full/v16/i3/92003.htm
- DOI: https://dx.doi.org/10.4239/wjd.v16.i3.92003